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Effect of transcranial direct current stimulation on postoperative delirium in elderly patients undergoing hip and knee arthroplasty

Effect of transcranial direct current stimulation on postoperative delirium in elderly patients undergoing hip and knee arthroplasty

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057024
Enrollment
Unknown
Registered
2022-02-26
Start date
2022-03-07
Completion date
Unknown
Last updated
2023-09-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

postoperative delirium

Interventions

experimental group:Transcranial direct current stimulation was performed. The left dorsolateral prefrontal lobe was stimulated by the anode, and the right supraorbital was stimulated by the cathode. T

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=65 years; 2. An elective knee or hip replacement is planned; 3. ASA grade was II -III; 4. The anesthesia method is intravenous inhalation combined anesthesia.

Exclusion criteria

Exclusion criteria: 1. Refuse to sign the test consent; 2. Have neuropsychiatric diseases, and have a history of neurological or psychiatric diseases; 3. Injuries with craniocerebral or cephalic lesions; 4. Visual and hearing impairment and difficulty in communication; 5. Serious cardiovascular and cerebrovascular diseases; 6. Patients with metal implants in the body; 7. Substance or alcohol abusers; 8. The score of Simple Mental Scale (MMSE) is less than 15 points; 9. With severe liver and kidney dysfunction (such as severe hepatitis, kidney failure).

Design outcomes

Primary

MeasureTime frame
Postoperative delirium;

Secondary

MeasureTime frame
Pain;Anxiety;Depression;Fatigue;Quality of recovery score;

Countries

China

Contacts

Public ContactCao Junli

Xuzhou Medical University

caojl0310@aliyun.com+86 15162160809

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026